Source: GWASCAT ×
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs4354968
rs4354968
2 16 76434236 intron variant T/A;C snv 0.700 1.000 1 2019 2019
dbSNP: rs58296637
rs58296637
2 16 76430039 intron variant G/C snv 2.2E-02 0.700 1.000 1 2015 2015